Switchable synthesis of glycosyl selenides or diselenides with direct use of selenium as the selenating agent-Reference-Cited by-同舟云学术

Switchable synthesis of glycosyl selenides or diselenides with direct use of selenium as the selenating agent

Published:2021 Issue:8 Volume:8 Page:1823-1829
ISSN:2052-4129
Container-title:Organic Chemistry Frontiers
language:en
Short-container-title:Org. Chem. Front.

Author:

Iadonisi Alfonso¹²³⁴^ORCID,Traboni Serena¹²³⁴^ORCID,Capasso Domenica⁵²⁶⁴,Bedini Emiliano¹²³⁴^ORCID,Cuomo Sabrina¹²³⁴,Di Gaetano Sonia⁷⁶⁴,Vessella Giulia¹²³⁴^ORCID

Affiliation:

1. Department of Chemical Sciences

2. University of Naples Federico II

3. 80126 Naples

4. Italy

5. Department of Pharmacy

6. 80134 Naples

7. Institute of Biostructures and Bioimaging-CNR

Abstract

Chemoselective synthesis of either diglycosyl selenides or diselenides. Elementary selenium as the selenating agent.

Funder

Università degli Studi di Napoli Federico II

Ministero dell’Istruzione, dell’Università e della Ricerca

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2021/QO/D1QO00045D

Reference32 articles.

1. Thiodigalactoside inhibits murine cancers by concurrently blocking effects of galectin-1 on immune dysregulation, angiogenesis and protection against oxidative stress

2. C2-Symmetrical Thiodigalactoside Bis-Benzamido Derivatives as High-Affinity Inhibitors of Galectin-3: Efficient Lectin Inhibition through Double Arginine-Arene Interactions

3. Galectins as modulators of tumour progression

4. Galectin–Carbohydrate Interactions in Biomedicine and Biotechnology

5. A straightforward synthetic access to symmetrical glycosyl disulfides and biological evaluation thereof

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